rs3850641, TNFSF4

N. diseases: 17
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.060 1.000 6 2005 2019
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.020 1.000 2 2011 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.020 1.000 2 2018 2019
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2019 2019
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2013 2013
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2013 2013
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2012 2012
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2012 2012
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2013 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2018 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2018 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1 2018 2018
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2016 2016
Hyperlipoproteinemia Type I
CUI: C0023817
Disease: Hyperlipoproteinemia Type I
64 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2013 2013
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2016 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2012 2012
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.716 0.400 1 173206693 intron variant A/G snv 0.14 0.010 1.000 1 2008 2008